Canonical Allele Identifier: CA2318945578
Gene: TBXA2R HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.3595351C= , CM000681.2:g.3595351C= GRCh38
NC_000019.9:g.3595349C= , CM000681.1:g.3595349C= GRCh37
NC_000019.8:g.3546349C= NCBI36
NG_013363.1:g.16483G= , LRG_578:g.16483G=
NG_031943.1:g.14781C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000375190.10:c.*337G= MANE Select ENSP00000364336.4:n.*337G=
ENST00000375190.8:c.*337G= ENSP00000364336.3:n.*337G=
ENST00000411851.3:c.984-275G= ENSP00000393333.2:n.984-275G=
ENST00000589966.1:c.*200G= ENSP00000468145.1:n.*200G=
NM_001060.5:c.*337G= , LRG_578t1:c.*337G= NP_001051.1:n.*337G=
NM_201636.2:c.984-275G= NP_963998.2:n.984-275G=
NM_001060.6:c.*337G= MANE Select NP_001051.1:n.*337G=
NM_201636.3:c.984-275G= NP_963998.2:n.984-275G=